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NCT04041583 · ClinicalTrials.gov registry record

Clinical and Radiological Outcomes of Posterior Cervical Fusion Supplemented With Interfacet Spacers

A clinical trial of Cervical Fusion, sponsored by Ohio State University.

Recruiting
Registry status
45
Enrollment target
1
Study location

NCT04041583 is a study of Cervical Fusion that is actively recruiting participants, run by Ohio State University. The registered enrollment target is 45 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT04041583, a study of Cervical Fusion, is actively recruiting participants, sponsored by Ohio State University.

RECRUITING
Registry status
45 participants
Enrollment target
1
Study location

Study Summary

This is a prospective study to assess fusion rates and cervical sagittal parameters following posterior cervical arthrodesis procedures supplemented with CIS. Data will be collected from medical records for up to 730 days after surgery. Data to be collected will be demographic, preoperative clinical information, surgical details, and radiographic information. Patients will also undergo a non-standard of care CT scan 2 years after surgery.

Conditions Studied

Interventions

  • DEVICE Cervical Interfacet Spacers

Study Locations (1)

Ohio

  • The Ohio State University Wexner Medical Center - Columbus

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2019-09-01
Est. Completion 2026-08

Sponsor

Ohio State University

552 total trials

What the Registry Record Tells You About NCT04041583

The ClinicalTrials.gov registry entry for NCT04041583 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ohio State University, which has 552 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Cervical Fusion appearing as the primary indexed condition, and to 1 intervention - of which Cervical Interfacet Spacers is the first listed.

NCT04041583 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT04041583 about?

NCT04041583 is a clinical study titled "Clinical and Radiological Outcomes of Posterior Cervical Fusion Supplemented With Interfacet Spacers". This is a prospective study to assess fusion rates and cervical sagittal parameters following posterior cervical arthrodesis procedures supplemented with CIS. Data will be collected from medical records for up to 730 days after surgery. Data to be collected will be demographic, preoperative clinical...

What is the current status of trial NCT04041583?

This trial is currently recruiting. The enrollment target is 45 participants. The study started on 2019-09-01. Estimated completion is 2026-08.

What conditions does trial NCT04041583 study?

This clinical trial studies the following conditions: Cervical Fusion.

What interventions are being tested in trial NCT04041583?

The interventions under investigation include: Cervical Interfacet Spacers (DEVICE).

Who is sponsoring clinical trial NCT04041583?

This trial is sponsored by Ohio State University, which has 552 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04041583 being conducted?

This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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